the silver bullet 10x Capsules — Class I drug recall D-0500-2019
Terminated recall by Natures Rx, reported 2019-02-13. Marketed without an Approved NDA/ANDA; FDA analysis found product to be tainted with undeclared sildenafil and
| Recall number | D-0500-2019 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Natures Rx, Claremont, CA, United States |
| Recall initiated | 2019-01-25 |
| Classified | 2019-02-15 |
| Reported by FDA | 2019-02-13 |
| Terminated | 2023-02-06 |
| Quantity | 211 |
| Reason classes | undeclared allergen, unapproved product |
Product
the silver bullet 10x Capsules, 725 mg each (proprietary blend of: Mucuna Pruriens Extract, Horny Goat Weed, Ginger Root Extract, Icariin, Wolf Berry (fruit) Lactase, Tribulus Terrestris Extract, Piperine), 10 count mylar package, Nature's Rx, Claremont, CA
Reason for recall
Marketed without an Approved NDA/ANDA; FDA analysis found product to be tainted with undeclared sildenafil and tadalafil
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0500-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.